Crystalline forms of N-[2-(3-Hydroxy-3-methylbutyl)-6-(2-hydroxypropan-2-yl)-2H-indazol-5-yl]-6-(trifluoromethyl)pyridine-2-carboxamide

US10501437B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10501437-B2
Application numberUS-201716097506-A
CountryUS
Kind codeB2
Filing dateApr 25, 2017
Priority dateApr 29, 2016
Publication dateDec 10, 2019
Grant dateDec 10, 2019

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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Abstract

Official abstract text for this publication.

The present invention relates to crystalline forms of N-[2-(3-Hydroxy-3-methylbutyl)-6-(2-hydroxypropan-2-yl)-2H-indazol-5-yl]-6-(trifluoromethyl)pyridine-2-carboxamide, to processes for their preparation, to pharmaceutical compositions comprising them and to their use in the control of disorders.

First claim

Opening claim text (preview).

The invention claimed is: 1. A hydrate of the compound of formula (I) wherein the hydrate has a X-ray powder diffraction diagram at 25° C. and with Cu-K alpha 1 as radiation source displaying at least the following reflections, quoted as 2Theta value ±0.2°: 9.4, 10.8, and 15.0. 2. The hydrate of the compound of formula (I) of claim 1 , wherein the hydrate has a X-ray powder diffraction diagram at 25° C. and with Cu-K alpha 1 as radiation source displaying at least the following reflections, quoted as 2Theta value ±0.2°: 9.4, 10.8, 15.0, 16.0, and 17.0. 3. The hydrate of the compound of formula (I) of claim 1 , wherein the hydrate has a X-ray powder diffraction diagram at 25° C. and with Cu-K alpha 1 as radiation source displaying at least the following reflections, quoted as 2Theta value ±0.2°: 9.4, 10.8, 15.0, 16.0, 17.0, 20.1, and 22.9. 4. The hydrate of the compound of formula (I) of claim 1 , wherein the hydrate has a X-ray powder diffraction diagram at 25° C. and with Cu-K alpha 1 as radiation source displaying at least the following reflections, quoted as 2Theta value ±0.2°: 9.4, 10.8, 15.0, 16.0, 17.0, 20.1, 22.9, 24.3, 26.6, and 29.8. 5. A pharmaceutical composition comprising only a hydrate of the compound of formula (I) according to claim 1 mainly and no significant fractions of another form of the compound of formula (I). 6. A pharmaceutical composition comprising a hydrate of the compound of formula (I) according to claim 1 and pharmaceutically acceptable excipients. 7. The pharmaceutical composition of claim 6 , comprising only the hydrate of the compound of formula (I) mainly and no significant fractions of another form of the compound of formula (I). 8. The pharmaceutical composition of claim 6 , comprising the hydrate of the compound of formula (I) in more than 85 percent by weight related to the total amount of all forms of the compound of the formula (I) present in the composition. 9. The pharmaceutical composition of claim 8 , comprising the hydrate of the compound of formula (I) in more than 90 percent by weight related to the total amount of all forms of the compound of formula (I) present in the composition. 10. A method for treatment of rheumatoid arthritis in a human in need thereof, comprising administering to the human an effective amount of a hydrate of the compound of formula (I) according to claim 1 . 11. A method for treatment of rheumatoid arthritis in a human in need thereof, comprising administering to the human an effective amount of a pharmaceutical composition according to claim 5 . 12. A method for treatment of rheumatoid arthritis in a human in need thereof, comprising administering to the human an effective amount of a pharmaceutical composition according to claim 6 .

Assignees

Inventors

Classifications

  • Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

  • Immunosuppressants, e.g. drugs for graft rejection · CPC title

  • Immunostimulants · CPC title

  • Immunomodulators · CPC title

  • Drugs for immunological or allergic disorders · CPC title

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Frequently asked questions

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What does patent US10501437B2 cover?
The present invention relates to crystalline forms of N-[2-(3-Hydroxy-3-methylbutyl)-6-(2-hydroxypropan-2-yl)-2H-indazol-5-yl]-6-(trifluoromethyl)pyridine-2-carboxamide, to processes for their preparation, to pharmaceutical compositions comprising them and to their use in the control of disorders.
Who is the assignee on this patent?
Bayer Pharma AG
What technology area does this patent fall under?
Primary CPC classification A61P35/00. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Dec 10 2019 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 10 related publications on this page (citations in our corpus or others sharing the same primary CPC).